Canonical Allele Identifier: CA1039047790
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1686253071
gnomAD v3: 2-169154296-CA-C
gnomAD v4: 2-169154296-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154298del , CM000664.2:g.169154298del GRCh38
NC_000002.11:g.170010808del , CM000664.1:g.170010808del GRCh37
NC_000002.10:g.169719054del NCBI36
NG_012634.1:g.213316del

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+163del MANE Select ENSP00000496870.1:n.12295+163del
ENST00000649153.1:c.3195+163del
ENST00000650252.1:c.1323+163del ENSP00000496887.1:n.1323+163del
ENST00000263816.7:c.12295+163del ENSP00000263816.3:n.12295+163del
NM_004525.2:c.12295+163del NP_004516.2:n.12295+163del
XM_011511183.1:c.12166+163del XP_011509485.1:n.12166+163del
XM_011511184.1:c.10006+163del XP_011509486.1:n.10006+163del
NM_004525.3:c.12295+163del MANE Select NP_004516.2:n.12295+163del
XM_011511183.3:c.12166+163del XP_011509485.1:n.12166+163del
XM_011511184.2:c.10006+163del XP_011509486.1:n.10006+163del
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